EP3495358B8 - Amide-substituted heterocyclic compounds useful as modulators of il-12, il-23 and/or ifn alpha responses - Google Patents

Amide-substituted heterocyclic compounds useful as modulators of il-12, il-23 and/or ifn alpha responses Download PDF

Info

Publication number
EP3495358B8
EP3495358B8 EP18197550.9A EP18197550A EP3495358B8 EP 3495358 B8 EP3495358 B8 EP 3495358B8 EP 18197550 A EP18197550 A EP 18197550A EP 3495358 B8 EP3495358 B8 EP 3495358B8
Authority
EP
European Patent Office
Prior art keywords
modulators
amide
substituted heterocyclic
heterocyclic compounds
compounds useful
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
EP18197550.9A
Other languages
German (de)
English (en)
French (fr)
Other versions
EP3495358B1 (en
EP3495358A1 (en
Inventor
Ryan M. MOSLIN
David S. Weinstein
Stephen T. Wrobleski
John S. Tokarski
Amit Kumar
Douglas G. Batt
Shuqun Lin
Chunjian Liu
Steven H. Spergel
Yanlei Zhang
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Bristol Myers Squibb Co
Original Assignee
Bristol Myers Squibb Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=49876960&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=EP3495358(B8) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Priority to RS20220589A priority Critical patent/RS63328B1/sr
Priority to PL18197550T priority patent/PL3495358T3/pl
Priority to HRP20220766TT priority patent/HRP20220766T1/hr
Priority to SI201331986T priority patent/SI3495358T1/sl
Priority to SM20220258T priority patent/SMT202200258T1/it
Application filed by Bristol Myers Squibb Co filed Critical Bristol Myers Squibb Co
Priority to EP22165094.8A priority patent/EP4071144A1/en
Publication of EP3495358A1 publication Critical patent/EP3495358A1/en
Publication of EP3495358B1 publication Critical patent/EP3495358B1/en
Publication of EP3495358B8 publication Critical patent/EP3495358B8/en
Application granted granted Critical
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/12Drugs for disorders of the urinary system of the kidneys
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/06Antipsoriatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • A61P37/06Immunosuppressants, e.g. drugs for graft rejection
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B59/00Introduction of isotopes of elements into organic compounds ; Labelled organic compounds per se
    • C07B59/002Heterocyclic compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D237/00Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
    • C07D237/02Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
    • C07D237/06Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D237/10Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D237/24Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/05Isotopically modified compounds, e.g. labelled

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Immunology (AREA)
  • Rheumatology (AREA)
  • Dermatology (AREA)
  • Urology & Nephrology (AREA)
  • Pain & Pain Management (AREA)
  • Diabetes (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Transplantation (AREA)
  • Hematology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Epidemiology (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Peptides Or Proteins (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
EP18197550.9A 2012-11-08 2013-11-07 Amide-substituted heterocyclic compounds useful as modulators of il-12, il-23 and/or ifn alpha responses Active EP3495358B8 (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
PL18197550T PL3495358T3 (pl) 2012-11-08 2013-11-07 Podstawione amidem związki heterocykliczne przydatne jako modulatory odpowiedzi il-12, il-23 i/lub ifn-alfa
HRP20220766TT HRP20220766T1 (hr) 2012-11-08 2013-11-07 Amidom-supstituirani heterociklički spojevi korisni kao modulatori il-12, il-23 i/ili ifn alfa odgovora
SI201331986T SI3495358T1 (sl) 2012-11-08 2013-11-07 z amidi substituirane heterociklične spojine, uporabne kot modulatorji IL-12, IL-23 in/ali IFN alfa odzivov
SM20220258T SMT202200258T1 (it) 2012-11-08 2013-11-07 Composti eterociclici ammido-sostituiti utili come modulatori delle risposte di il-12, il-23 e/o ifn-a
RS20220589A RS63328B1 (sr) 2012-11-08 2013-11-07 Amidom-supstituisana heterociklična jedinjenja korisna kao modulatori il-12, il-23 i/ili ifn alfa odgovora
EP22165094.8A EP4071144A1 (en) 2012-11-08 2013-11-07 Amide-substituted heterocyclic compounds useful as modulators of il-12, il-23 and/or ifn alpha responses

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201261723840P 2012-11-08 2012-11-08
EP13811640.5A EP2922846B1 (en) 2012-11-08 2013-11-07 Amide-substituted heterocyclic compounds useful as modulators of il-12, il-23 and/or ifn-alpha
PCT/US2013/068846 WO2014074661A1 (en) 2012-11-08 2013-11-07 AMIDE-SUBSTITUTED HETEROCYCLIC COMPOUNDS USEFUL AS MODULATORS OF IL-12, IL-23 AND/OR IFN ALPHα RESPONSES

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
EP13811640.5A Division EP2922846B1 (en) 2012-11-08 2013-11-07 Amide-substituted heterocyclic compounds useful as modulators of il-12, il-23 and/or ifn-alpha

Related Child Applications (2)

Application Number Title Priority Date Filing Date
EP22165094.8A Division EP4071144A1 (en) 2012-11-08 2013-11-07 Amide-substituted heterocyclic compounds useful as modulators of il-12, il-23 and/or ifn alpha responses
EP22165094.8A Division-Into EP4071144A1 (en) 2012-11-08 2013-11-07 Amide-substituted heterocyclic compounds useful as modulators of il-12, il-23 and/or ifn alpha responses

Publications (3)

Publication Number Publication Date
EP3495358A1 EP3495358A1 (en) 2019-06-12
EP3495358B1 EP3495358B1 (en) 2022-04-27
EP3495358B8 true EP3495358B8 (en) 2022-06-08

Family

ID=49876960

Family Applications (3)

Application Number Title Priority Date Filing Date
EP18197550.9A Active EP3495358B8 (en) 2012-11-08 2013-11-07 Amide-substituted heterocyclic compounds useful as modulators of il-12, il-23 and/or ifn alpha responses
EP22165094.8A Pending EP4071144A1 (en) 2012-11-08 2013-11-07 Amide-substituted heterocyclic compounds useful as modulators of il-12, il-23 and/or ifn alpha responses
EP13811640.5A Active EP2922846B1 (en) 2012-11-08 2013-11-07 Amide-substituted heterocyclic compounds useful as modulators of il-12, il-23 and/or ifn-alpha

Family Applications After (2)

Application Number Title Priority Date Filing Date
EP22165094.8A Pending EP4071144A1 (en) 2012-11-08 2013-11-07 Amide-substituted heterocyclic compounds useful as modulators of il-12, il-23 and/or ifn alpha responses
EP13811640.5A Active EP2922846B1 (en) 2012-11-08 2013-11-07 Amide-substituted heterocyclic compounds useful as modulators of il-12, il-23 and/or ifn-alpha

Country Status (39)

Country Link
US (7) US9505748B2 (OSRAM)
EP (3) EP3495358B8 (OSRAM)
JP (3) JP6407159B2 (OSRAM)
KR (1) KR102195194B1 (OSRAM)
CN (1) CN104884454B (OSRAM)
AR (1) AR094452A1 (OSRAM)
AU (4) AU2013341186B2 (OSRAM)
BR (1) BR112015010102B1 (OSRAM)
CA (1) CA2890981C (OSRAM)
CL (1) CL2015001231A1 (OSRAM)
CY (3) CY1121188T1 (OSRAM)
DK (2) DK2922846T3 (OSRAM)
EA (1) EA028814B1 (OSRAM)
ES (2) ES2914793T3 (OSRAM)
FI (1) FIC20230028I1 (OSRAM)
FR (1) FR23C1030I2 (OSRAM)
HR (2) HRP20220766T1 (OSRAM)
HU (3) HUE059409T2 (OSRAM)
IL (1) IL238610A0 (OSRAM)
LT (3) LT3495358T (OSRAM)
MA (1) MA38072A1 (OSRAM)
MX (2) MX2015005731A (OSRAM)
MY (3) MY194668A (OSRAM)
NL (1) NL301238I2 (OSRAM)
NO (1) NO2023032I1 (OSRAM)
NZ (1) NZ708859A (OSRAM)
PE (1) PE20150944A1 (OSRAM)
PH (1) PH12015501004B1 (OSRAM)
PL (2) PL2922846T3 (OSRAM)
PT (2) PT2922846T (OSRAM)
RS (2) RS63328B1 (OSRAM)
SG (3) SG11201503399XA (OSRAM)
SI (2) SI2922846T1 (OSRAM)
SM (2) SMT201900001T1 (OSRAM)
TR (1) TR201820824T4 (OSRAM)
TW (1) TWI605041B (OSRAM)
UY (1) UY35126A (OSRAM)
WO (1) WO2014074661A1 (OSRAM)
ZA (1) ZA201504052B (OSRAM)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US12084458B2 (en) 2021-02-19 2024-09-10 Sudo Biosciences Limited Substituted pyridines, pyridazines, and pyrimidines as TYK2 inhibitors
US12122785B2 (en) 2021-02-19 2024-10-22 Sudo Biosciences Limited Substituted pyridines, pyridazines, pyrimidines, and 1,2,4-triazines as TYK2 inhibitors

Families Citing this family (113)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9540333B2 (en) 2012-11-08 2017-01-10 Bristol-Myers Squibb Company Alkyl amide-substituted pyrimidine compounds useful in the modulation of IL-12, IL-23 and/or IFNα
WO2014074661A1 (en) * 2012-11-08 2014-05-15 Bristol-Myers Squibb Company AMIDE-SUBSTITUTED HETEROCYCLIC COMPOUNDS USEFUL AS MODULATORS OF IL-12, IL-23 AND/OR IFN ALPHα RESPONSES
AR094537A1 (es) 2013-11-07 2015-08-12 Bristol Myers Squibb Co COMPUESTOS DE PIRIDILO SUSTITUIDOS CON ALQUILAMIDA ÚTILES COMO MODULADORES DE LAS RESPUESTAS DE IL-12, IL-23 Y/O IFNa
WO2015089143A1 (en) 2013-12-10 2015-06-18 Bristol-Myers Squibb Company Imidazopyridazine compounds useful as modulators of il-12, il-23 and/or ifn alpha responses
WO2015123453A1 (en) * 2014-02-14 2015-08-20 Portola Pharmaceuticals, Inc. Pyridazine compounds as jak inhibitors
PE20181071A1 (es) 2015-11-26 2018-07-04 Novartis Ag Derivados novedosos de diamino piridina
TWI825663B (zh) 2016-10-14 2023-12-11 美商林伯士拉克許米公司 Tyk2抑制劑及其用途
AU2017345736B2 (en) 2016-10-21 2022-04-07 Takeda Pharmaceutical Company Limited TYK2 inhibitors and uses thereof
ES2907008T3 (es) * 2016-12-13 2022-04-21 Bristol Myers Squibb Co Compuestos de heteroarilo sustituidos con fosfinóxido alquilamida como moduladores de respuestas de IL-12, IL-23 y/o IFN alfa
JOP20180011A1 (ar) 2017-02-16 2019-01-30 Gilead Sciences Inc مشتقات بيرولو [1، 2-b]بيريدازين
JP7160824B2 (ja) 2017-03-08 2022-10-25 ニンバス ラクシュミ, インコーポレイテッド Tyk2阻害剤、使用およびその製造のための方法
WO2018183656A1 (en) * 2017-03-30 2018-10-04 Bristol-Myers Squibb Company Crystal form of 6-(cyclopropanecarboxamido)-4-((2-methoxy-3-(1-methyl-1h-1,2,4-triazol-3-yl)phenyl)amino)-n-(methyl-d3) pyridazine-3-carboxamide
EP3713930A1 (en) * 2017-11-21 2020-09-30 Bristol-Myers Squibb Company Sulfone pyridine alkyl amide-substituted heteroaryl compounds
UY38144A (es) 2018-03-12 2019-10-31 Abbvie Inc Inhibidores de la señalización mediada por tirosina cinasa
CN111936486B (zh) * 2018-03-22 2023-09-22 百时美施贵宝公司 用作IL-12、IL-23和/或IFNα响应的调节剂的包含吡啶的杂环化合物
US11613529B2 (en) 2018-05-31 2023-03-28 Bristol-Myers Squibb Company Crystalline form of 6-(cyclopropanecarboxamido)-4-((2-methoxy-3-(1-methyl-1H-1,2,4-triazol-3-yl)phenyl)amino)-N-(methyl-D3) pyridazine-3-carboxamide
TWI721483B (zh) 2018-07-13 2021-03-11 美商基利科學股份有限公司 吡咯并[1,2-b]嗒𠯤衍生物
GB201816369D0 (en) 2018-10-08 2018-11-28 Sareum Ltd Pharmaceutical compounds
CN113271940A (zh) 2018-10-15 2021-08-17 林伯士拉克许米公司 Tyk2抑制剂和其用途
FI3870579T3 (fi) * 2018-10-22 2025-01-02 Alumis Inc Tyk2-inhibiittoreita ja niiden käyttöjä
AU2019373203B2 (en) * 2018-10-30 2024-10-24 Bristol-Myers Squibb Company Amide-substituted heterocyclic compounds for the treatment of conditions related to the modulation of IL-12, IL-23 and/or IFN-alpha
CA3120866A1 (en) 2018-11-30 2020-06-04 Nimbus Lakshmi, Inc. Tyk2 inhibitors and uses thereof
EP3914357A4 (en) 2019-01-23 2022-10-12 Nimbus Lakshmi, Inc. TYK2 INHIBITORS AND THEIR USES
KR20210119426A (ko) * 2019-01-28 2021-10-05 장쑤 한서 파마슈티칼 그룹 캄파니 리미티드 피리다진 유도체 억제제, 및 그의 제조 방법 및 용도
CN111484480B (zh) * 2019-01-29 2023-08-11 上海翰森生物医药科技有限公司 一种多环类衍生物抑制剂、其制备方法和应用
ES3035735T3 (en) * 2019-01-30 2025-09-08 Bristol Myers Squibb Co Amide-disubstituted pyridine or pyridazine compounds
US11357775B2 (en) 2019-04-30 2022-06-14 Celgene Corporation Combination therapies comprising apremilast and Tyk2 inhibitors
IL287665A (en) 2019-04-30 2022-07-01 Celgene Corp Combined treatments including apremilaste and tyk2 inhibitors
CN114174284A (zh) * 2019-06-12 2022-03-11 百时美施贵宝公司 6-(环丙烷甲酰胺基)-4-((2-甲氧基-3-(1-甲基-1H-1,2,4-三唑-3-基)苯基)氨基)-N-(甲基-d3)哒嗪-3-甲酰胺的结晶盐形式
ES2991171T3 (es) * 2019-07-16 2024-12-02 Bristol Myers Squibb Co Profármacos en la modulación de la interleucina
US12428395B2 (en) 2019-08-01 2025-09-30 Sperogenix Therapeutics Limited Heterocyclic compounds as kinase inhibitor and uses thereof
BR112022004451A2 (pt) 2019-09-13 2022-06-21 Nimbus Saturn Inc Antagonistas de hpk1 e usos dos mesmos
CN119424435A (zh) 2019-09-18 2025-02-14 百时美施贵宝公司 Tyk2抑制剂的剂型
CN114787152A (zh) * 2019-12-27 2022-07-22 苏州科睿思制药有限公司 一种bms-986165晶型及其制备方法和用途
CN114787154A (zh) * 2020-01-19 2022-07-22 苏州科睿思制药有限公司 一种Deucravacitinib的晶型及其制备方法和用途
WO2021143430A1 (zh) * 2020-01-19 2021-07-22 苏州科睿思制药有限公司 一种bms-986165盐酸盐晶型及其制备方法和用途
WO2021170046A1 (en) * 2020-02-26 2021-09-02 Beigene, Ltd. Tyk-2 inhibitor
PT4038063T (pt) 2020-03-11 2024-05-22 Beijing Innocare Pharma Tech Co Ltd Compostos heterocíclicos para inibição de atividades de tyk2
WO2021204626A1 (en) * 2020-04-06 2021-10-14 Almirall, S.A. Aryl and heteroaryl-carboxamide substituted heteroaryl compounds as tyk2 inhibitors
GB202005114D0 (en) 2020-04-07 2020-05-20 Sareum Ltd Crystalline Forms of a Pharmaceutical Compound
CN113563309B (zh) * 2020-04-28 2024-12-13 浙江海正药业股份有限公司 吡啶类衍生物及其制备方法和用途
EP4143180A1 (en) * 2020-04-28 2023-03-08 Bristol-Myers Squibb Company Substituted n-(methyl-d3)pyridazine-3-carboxamide or n-(methyl-d3)-nicotinamide compounds as il-12, il-23 and/or ifnalpha modulators
CN113735837B (zh) * 2020-05-28 2023-09-01 江苏先声药业有限公司 哒嗪类化合物及其用途
CN113735836B (zh) * 2020-05-28 2023-05-30 江苏先声药业有限公司 哒嗪类化合物及其应用
CN113773262B (zh) * 2020-06-09 2024-08-09 江苏先声药业有限公司 哒嗪类化合物
CN115715288B (zh) 2020-06-22 2025-11-25 百济神州有限公司 Tyk-2抑制剂
CA3186000A1 (en) * 2020-07-24 2022-01-27 Shanghai Hansoh Biomedical Co., Ltd. Crystal form of pyridazine derivative free base, and preparation method therefor and use thereof
CN113968846A (zh) * 2020-07-24 2022-01-25 上海翰森生物医药科技有限公司 一种哒嗪类衍生物的盐、晶型及其制备方法和应用
EP3944859A1 (en) 2020-07-30 2022-02-02 Assistance Publique Hôpitaux de Paris Method for treating immune toxicities induced by immune checkpoint inhibitors
CN114057651B (zh) * 2020-07-31 2025-05-27 正大天晴药业集团股份有限公司 含酰胺基的tyk2抑制剂化合物
WO2022021684A1 (zh) * 2020-07-31 2022-02-03 苏州科睿思制药有限公司 一种bms-986165盐酸盐晶型csv及其制备方法和用途
IL301389A (en) 2020-09-18 2023-05-01 Bristol Myers Squibb Co Dosage forms for tyk2 inhibitors comprising swellable cores
CN116615200B (zh) * 2020-10-20 2025-04-29 杭州领业医药科技有限公司 哒嗪衍生物的晶型
US12331046B2 (en) 2020-10-23 2025-06-17 Nimbus Clotho, Inc. CTPS1 inhibitors and uses thereof
WO2022100710A1 (en) * 2020-11-12 2022-05-19 Cullgen (Shanghai) , Inc. Tyrosine kinase 2 (tyk2) degradation compounds and methods of use
WO2022105771A1 (zh) * 2020-11-17 2022-05-27 江苏恒瑞医药股份有限公司 含氮杂环类衍生物、其制备方法及其在医药上的应用
CN116547276A (zh) * 2020-12-08 2023-08-04 正大天晴药业集团股份有限公司 含酰胺基和杂环烷基的tyk2抑制剂化合物
CN115160297B (zh) 2020-12-22 2023-03-31 益方生物科技(上海)股份有限公司 杂芳基化合物及其制备方法和用途
EP4284796B1 (en) * 2021-01-29 2025-04-16 Bristol-Myers Squibb Company Crystal form of 6-(cyclopropanecarboxamido)-4-((2-methoxy-3-(1-methyl-1h-1,2,4-triazol-3-yl)phenyl)amino)-n-(methyl-d3)pyridazine-3-carboxamide
CA3206501A1 (en) 2021-02-02 2022-08-11 Shaun Abbott Gpr84 antagonists and uses thereof
CA3206499A1 (en) 2021-02-02 2022-08-11 Liminal Biosciences Limited Gpr84 antagonists and uses thereof
TW202233600A (zh) * 2021-02-06 2022-09-01 大陸商正大天晴藥業集團股份有限公司 含聯環的tyk2抑制劑化合物、藥物組合物及其用途
CN114907326B (zh) * 2021-02-06 2025-02-18 正大天晴药业集团股份有限公司 含酰胺基和联环的tyk2抑制剂化合物
CN117120090A (zh) 2021-02-12 2023-11-24 林伯士萨顿公司 Hpk1拮抗剂和其用途
JP2024509192A (ja) 2021-03-05 2024-02-29 ニンバス サターン, インコーポレイテッド Hpk1アンタゴニスト及びその使用
WO2022193499A1 (en) 2021-03-16 2022-09-22 Anrui Biomedical Technology (Guangzhou) Co., Ltd. Amino heteroaryl compounds and compositions
JP2024513011A (ja) 2021-03-29 2024-03-21 ニンバス サターン, インコーポレイテッド Hpk1アンタゴニスト及びその使用
EP4313974A1 (en) 2021-03-29 2024-02-07 Bristol-Myers Squibb Company Crystal forms of 6-(cyclopropanecarboxamido)-4-((2-methoxy-3-(1-methyl-1h-1,2,4-triazol-3-yl)phenyl)amino)-n-(methyl-d3)pyridazine-3-carboxamide
CN117177960B (zh) * 2021-03-30 2025-01-28 浙江文达医药科技有限公司 作为tyk2假激酶结构域抑制剂的杂环化合物及合成方法和用途
CN115197196B (zh) * 2021-04-06 2024-06-18 扬子江药业集团有限公司 Tyk2抑制剂及其用途
EP4319756A4 (en) 2021-04-09 2025-02-26 Nimbus Clio, Inc. CBL-B MODULATORS AND USES THEREOF
JP7740849B2 (ja) 2021-05-04 2025-09-17 シャンハイ ゼイ バイオテクノロジー カンパニー リミテッド 含窒素複素環ピリジン化合物
WO2022241175A1 (en) 2021-05-14 2022-11-17 Bristol-Myers Squibb Company Substituted heterocyclic compounds
EP4337649A1 (en) * 2021-05-14 2024-03-20 Bristol-Myers Squibb Company Substituted heterocyclic compounds
US20250066322A1 (en) 2021-05-14 2025-02-27 Bristol-Myers Squibb Company Substituted heterocyclic compounds
TW202311247A (zh) 2021-05-14 2023-03-16 美商必治妥美雅史谷比公司 經取代之雜環化合物
WO2022253335A1 (zh) * 2021-06-02 2022-12-08 南京明德新药研发有限公司 含磺酰基的芳基类化合物及其应用
CN115466289A (zh) * 2021-06-11 2022-12-13 爱科诺生物医药(香港)有限公司 具有tyk2抑制活性的化合物,包含其的药物组合物,及其应用
US20240376093A1 (en) * 2021-06-22 2024-11-14 Medshine Discovery Inc. Sulfoximine compound and use thereof
EP4371981A1 (en) * 2021-07-15 2024-05-22 Medshine Discovery Inc. Sulfur/phosphorus-containing aryl compound and application thereof
KR20240050380A (ko) * 2021-08-20 2024-04-18 브리스톨-마이어스 스큅 컴퍼니 6-(시클로프로판카르복스아미도)-4-((2-메톡시-3-(1-메틸-1h-1,2,4-트리아졸-3-일)페닐)아미노)-n-(메틸-d3)피리다진-3-카르복스아미드의결정 형태
TW202313035A (zh) * 2021-08-21 2023-04-01 美商傳達治療有限公司 Jak2抑制劑及其使用方法
EP4404930A1 (en) 2021-09-23 2024-07-31 Bristol-Myers Squibb Company Methods of treating hair-loss disorders with tyk2 inhibitors
US20240390369A1 (en) 2021-09-30 2024-11-28 Bristol-Myers Squibb Company Methods for determining responsiveness to tyk2 inhibitors
AU2022378463A1 (en) 2021-10-25 2024-05-09 Kymera Therapeutics, Inc. Tyk2 degraders and uses thereof
WO2023076515A1 (en) 2021-10-28 2023-05-04 Bristol-Myers Squibb Company Topical formulations of deucravacitinib
WO2023102085A1 (en) 2021-12-01 2023-06-08 Teva Czech Industries S.R.O. Solid state forms of deucravacitinib, deucravacitinib hcl and process for preparation of deucravacitinib and intermediates
WO2023108536A1 (en) * 2021-12-16 2023-06-22 Lynk Pharmaceuticals Co. Ltd. Tyk2 inhibitors and compositions and methods thereof
WO2023109954A1 (en) * 2021-12-16 2023-06-22 Lynk Pharmaceuticals Co. Ltd. Tyk2 inhibitors and compositions and methods thereof
CN116283928A (zh) * 2021-12-20 2023-06-23 艾立康药业股份有限公司 一种哒嗪类化合物、其制备方法和应用
EP4206196A1 (en) 2021-12-29 2023-07-05 Almirall S.A. Pyrimidine substituted derivatives as tyk2 inhibitors
CN116693449A (zh) * 2022-03-04 2023-09-05 上海致根医药科技有限公司 用作tyk2抑制剂的化合物、其制备方法及其在医药上的应用
CN119233971A (zh) * 2022-05-31 2024-12-31 上海华汇拓医药科技有限公司 一种哒嗪类化合物、其制备方法和用途
CN117447411B (zh) * 2022-07-18 2025-12-23 苏州鹏旭医药科技有限公司 一种杂环药物中间体的合成方法
WO2024020221A1 (en) 2022-07-21 2024-01-25 Arvinas Operations, Inc. Modulators of tyk2 proteolysis and associated methods of use
EP4565564A1 (en) 2022-08-02 2025-06-11 Liminal Biosciences Limited Substituted pyridone gpr84 antagonists and uses thereof
WO2024028364A1 (en) 2022-08-02 2024-02-08 Liminal Biosciences Limited Aryl-triazolyl and related gpr84 antagonists and uses thereof
AU2023317740A1 (en) 2022-08-02 2025-03-13 Liminal Biosciences Limited Heteroaryl carboxamide and related gpr84 antagonists and uses thereof
EP4615832A1 (en) 2022-11-08 2025-09-17 Bristol-Myers Squibb Company Substituted heterocyclic compounds
TW202430168A (zh) 2022-12-16 2024-08-01 印度商阿蘭比克製藥有限公司 Tyk2假激酶配體及其用途
CN116284040B (zh) * 2023-01-05 2024-05-28 华润医药研究院(深圳)有限公司 含氮杂环类化合物及其医药用途
CN120693328A (zh) * 2023-02-07 2025-09-23 浙江华海药业股份有限公司 一种哒嗪类化合物、其制备方法和用途
CN118724752B (zh) * 2023-03-29 2025-11-28 重庆博腾制药科技股份有限公司 一种酪氨酸激酶抑制剂中间体、制备方法及其应用
CN116162093B (zh) * 2023-04-25 2023-06-23 中南大学湘雅医院 一种tyk2抑制剂化合物及其用途
WO2024236491A1 (en) * 2023-05-15 2024-11-21 Glenmark Life Sciences Limited Process for the preparation of deucravacitinib, and crystalline forms thereof
CN119080742A (zh) * 2023-06-05 2024-12-06 甘莱制药有限公司 脂质合成的杂环调节剂的工业化制备
WO2024257023A1 (en) 2023-06-14 2024-12-19 Alembic Pharmaceuticals Limited Tyk2 pseudokinase ligands and uses thereof
WO2025062372A1 (en) 2023-09-21 2025-03-27 Takeda Pharmaceutical Company Limited Tyk2 inhibitors for use in the treatment of inflammatory bowel disease
EP4538259A1 (en) 2023-10-09 2025-04-16 Farmhispania Group, S.L. Processes for the preparation of deucravacitinib
WO2025131031A1 (zh) * 2023-12-22 2025-06-26 上海奥博生物医药股份有限公司 一种TyK2抑制剂及其中间体的制备方法
WO2025186427A1 (en) 2024-03-08 2025-09-12 Curia Spain, S.A.U. Process for the preparation of deucravacitinib and intermediates thereof and method for purifying deucravacitinib
CN118593504B (zh) * 2024-06-03 2025-03-18 北京大学第三医院(北京大学第三临床医学院) 氘可来昔替尼或其盐在制备pvns药物方面的新用途
CN119059972B (zh) * 2024-08-12 2025-10-28 武汉九州钰民医药科技有限公司 一种btk抑制剂吡托布鲁替尼的合成方法

Family Cites Families (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4622047B2 (ja) * 1999-06-09 2011-02-02 アステラス製薬株式会社 新規なヘテロ環カルボキサミド誘導体
DE60017898T2 (de) 1999-06-09 2006-01-12 Yamanouchi Pharmaceutical Co., Ltd. Neuartige heterocyclische carboxamidderivate
AU5108000A (en) * 1999-06-10 2001-01-02 Yamanouchi Pharmaceutical Co., Ltd. Novel nitrogen-contaiing heterocyclic derivatives or salts thereof
US7273868B2 (en) 2000-04-28 2007-09-25 Tanabe Seiyaku Co., Ltd. Pyrazine derivatives
CA2356544C (en) 2000-10-03 2006-04-04 Warner-Lambert Company Pyridotriazines and pyridopyridazines
AU2003251900B2 (en) 2002-07-15 2008-12-18 President And Fellows Of Harvard College Methods and compositions for modulating T helper (Th) cell development and function
US7176214B2 (en) 2003-05-21 2007-02-13 Bristol-Myers Squibb Company Imidazo-fused oxazolo[4,5-β]pyridine and imidazo-fused thiazolo[4,5-β]pyridine based tricyclic compounds and pharmaceutical compositions comprising same
RU2012141536A (ru) * 2010-03-17 2014-04-27 Ф. Хоффманн-Ля Рош Аг Имидазопиридины, композиции и способы применения
CN103209695A (zh) 2010-09-15 2013-07-17 弗·哈夫曼-拉罗切有限公司 氮杂苯并噻唑化合物、组合物及应用方法
KR20140009259A (ko) 2010-11-19 2014-01-22 에프. 호프만-라 로슈 아게 피라졸로피리딘 및 tyk2 억제제로서 이의 용도
JP5878178B2 (ja) * 2011-09-30 2016-03-08 大鵬薬品工業株式会社 1,2,4−トリアジン−6−カルボキサミド誘導体
CN104159891B (zh) * 2012-01-10 2016-09-07 霍夫曼-拉罗奇有限公司 哒嗪酰胺化合物和它们作为syk 抑制剂的用途
UY34807A (es) 2012-05-16 2013-12-31 Novartis Ag Derivados monocíclicos de heteroarilcicloalquil- diamina
US9040530B2 (en) * 2012-06-22 2015-05-26 Portola Pharmaceuticals, Inc. 1,2,4-triazine-6-carboxamide kinase inhibitors
CA2883534A1 (en) * 2012-10-19 2014-04-24 F. Hoffmann-La Roche Ag Inhibitors of syk
US9540333B2 (en) 2012-11-08 2017-01-10 Bristol-Myers Squibb Company Alkyl amide-substituted pyrimidine compounds useful in the modulation of IL-12, IL-23 and/or IFNα
WO2014074661A1 (en) * 2012-11-08 2014-05-15 Bristol-Myers Squibb Company AMIDE-SUBSTITUTED HETEROCYCLIC COMPOUNDS USEFUL AS MODULATORS OF IL-12, IL-23 AND/OR IFN ALPHα RESPONSES
TWI620737B (zh) 2012-11-08 2018-04-11 必治妥美雅史谷比公司 作爲IL-12、IL-23及/或IFNα反應調節劑之經烷基-醯胺取代之吡啶化合物
AR094537A1 (es) * 2013-11-07 2015-08-12 Bristol Myers Squibb Co COMPUESTOS DE PIRIDILO SUSTITUIDOS CON ALQUILAMIDA ÚTILES COMO MODULADORES DE LAS RESPUESTAS DE IL-12, IL-23 Y/O IFNa
WO2018183656A1 (en) * 2017-03-30 2018-10-04 Bristol-Myers Squibb Company Crystal form of 6-(cyclopropanecarboxamido)-4-((2-methoxy-3-(1-methyl-1h-1,2,4-triazol-3-yl)phenyl)amino)-n-(methyl-d3) pyridazine-3-carboxamide

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US12084458B2 (en) 2021-02-19 2024-09-10 Sudo Biosciences Limited Substituted pyridines, pyridazines, and pyrimidines as TYK2 inhibitors
US12103937B2 (en) 2021-02-19 2024-10-01 Sudo Biosciences Limited Substituted pyridines and pyridazines as TYK2 inhibitors
US12122785B2 (en) 2021-02-19 2024-10-22 Sudo Biosciences Limited Substituted pyridines, pyridazines, pyrimidines, and 1,2,4-triazines as TYK2 inhibitors

Also Published As

Publication number Publication date
EP3495358B1 (en) 2022-04-27
KR102195194B1 (ko) 2020-12-24
UY35126A (es) 2014-05-30
MY194668A (en) 2022-12-12
CY1121188T1 (el) 2020-05-29
CL2015001231A1 (es) 2015-08-28
ZA201504052B (en) 2017-11-29
US20180265504A1 (en) 2018-09-20
SI3495358T1 (sl) 2022-06-30
CY2023017I2 (el) 2024-02-16
JP2018154636A (ja) 2018-10-04
EP3495358A1 (en) 2019-06-12
JP2020002157A (ja) 2020-01-09
PL2922846T3 (pl) 2019-03-29
AU2013341186B2 (en) 2017-03-30
AR094452A1 (es) 2015-08-05
EA028814B1 (ru) 2018-01-31
US11021475B2 (en) 2021-06-01
FR23C1030I2 (fr) 2024-10-25
AU2018267545A1 (en) 2018-12-13
JP6407159B2 (ja) 2018-10-17
JP6585231B2 (ja) 2019-10-02
SI2922846T1 (sl) 2019-04-30
US20200071315A1 (en) 2020-03-05
HUS2300025I1 (hu) 2023-08-28
MX2020003156A (es) 2020-07-29
DK2922846T3 (en) 2019-01-21
PT3495358T (pt) 2022-06-02
SG10201706897TA (en) 2017-09-28
CY1125220T1 (el) 2025-03-28
TR201820824T4 (tr) 2019-01-21
SMT202200258T1 (it) 2022-07-21
IL238610A0 (en) 2015-06-30
CN104884454B (zh) 2017-11-28
AU2020203967A1 (en) 2020-07-16
DK3495358T3 (da) 2022-05-23
EP2922846A1 (en) 2015-09-30
TW201422593A (zh) 2014-06-16
PH12015501004A1 (en) 2015-07-27
US20150299183A1 (en) 2015-10-22
FR23C1030I1 (fr) 2023-10-13
AU2017201076A1 (en) 2017-03-09
AU2020203967B2 (en) 2020-10-22
EP4071144A1 (en) 2022-10-12
CY2023017I1 (el) 2023-11-15
LTC2922846I2 (OSRAM) 2024-10-25
PE20150944A1 (es) 2015-06-20
HRP20220766T1 (hr) 2022-09-16
EP2922846B1 (en) 2018-10-03
US10526321B2 (en) 2020-01-07
HRP20181937T1 (hr) 2019-01-25
NL301238I2 (nl) 2023-10-04
SG11201503399XA (en) 2015-05-28
CA2890981A1 (en) 2014-05-15
NZ708859A (en) 2018-11-30
AU2017201076B2 (en) 2018-11-15
MA38072A1 (fr) 2016-07-29
US20170022192A1 (en) 2017-01-26
RS58187B1 (sr) 2019-03-29
US9505748B2 (en) 2016-11-29
NO2023032I1 (en) 2023-08-25
MY198262A (en) 2023-08-17
HUE041750T2 (hu) 2019-05-28
PH12015501004B1 (en) 2015-07-27
RS63328B1 (sr) 2022-07-29
TWI605041B (zh) 2017-11-11
CA2890981C (en) 2022-07-05
MY175448A (en) 2020-06-29
LT3495358T (lt) 2022-05-25
US20250243193A1 (en) 2025-07-31
CN104884454A (zh) 2015-09-02
MX2015005731A (es) 2015-09-16
US20220356180A1 (en) 2022-11-10
WO2014074661A1 (en) 2014-05-15
ES2702148T3 (es) 2019-02-27
HUE059409T2 (hu) 2022-11-28
JP2016506369A (ja) 2016-03-03
BR112015010102B1 (pt) 2022-02-08
EA201590917A1 (ru) 2015-09-30
AU2013341186A1 (en) 2015-07-02
KR20150081339A (ko) 2015-07-13
USRE47929E1 (en) 2020-04-07
HK1215255A1 (en) 2016-08-19
US10000480B2 (en) 2018-06-19
AU2018267545B2 (en) 2020-04-02
LT2922846T (lt) 2018-12-10
PT2922846T (pt) 2018-12-19
BR112015010102A2 (pt) 2017-07-11
SG10201706985UA (en) 2017-10-30
SMT201900001T1 (it) 2019-02-28
LTPA2023523I1 (OSRAM) 2023-09-11
PL3495358T3 (pl) 2022-06-27
ES2914793T3 (es) 2022-06-16
FIC20230028I1 (fi) 2023-08-28

Similar Documents

Publication Publication Date Title
HUS2300025I1 (hu) Amidszubsztituált heterociklikus vegyületek mint IL-12, IL-23 és/vagy IFN-ALFA modulátorai
EP2922841B8 (en) Alkyl-amide-substituted pyridyl compounds useful as modulators of il-12, il-23 and/or ifn alpha responses
IL245448B (en) Alkyl-amide substituted pyridyl compounds useful as modulators of responses to il-12, il-23, and/or ifnalpha
EP3062796A4 (en) Compositions and methods for ophthalmic and/or other applications
EP3065875A4 (en) Bioprinter and methods of using same
EP3038634A4 (en) Novel sez6 modulators and methods of use
EP3054870A4 (en) Compressed bone composition and methods of use thereof
EP3086647A4 (en) Antimicrobial substrates and methods of use thereof
WO2015081319A3 (en) Activity enhancing curcumin compositions and methods of use
EP3050881A4 (en) Novel a-naphthylurea derivative and medical application of same
EP3049389A4 (en) Kynurenine-3-monooxygenase inhibitors, pharmaceutical compositions, and methods of use thereof
EP3082845A4 (en) Methods and compositions for treatment of peripheral neuropathies
EP3037099A4 (en) Pharmaceutical composition, preparation method therefor and use thereof
EP3049077A4 (en) Kynurenine-3-monooxygenase inhibitors, pharmaceutical compositions, and methods of use thereof
EP2900783A4 (en) DEHYDRATED GEL COMPOSITIONS AND USE METHOD THEREFOR
GB201307082D0 (en) Pharmaceutical composition comprising 15-HETrE and methods of using the same
AU2014318672B2 (en) Recombinant microorganisms and methods of use thereof
EP2874624B8 (en) Injectable antibiotic formulations and their methods of use
SMT201900406T1 (it) Composti piridilici alchil-ammide-sostitidti utili come modulatori delle risposte di il-12, il-23 e/o ifn-alfa
AU2013101402A4 (en) Timber treatment formulations and methods of use
AU2013902122A0 (en) Ectoparasitic Treatment Method and Composition

Legal Events

Date Code Title Description
REG Reference to a national code

Ref country code: HR

Ref legal event code: TUEP

Ref document number: P20220766T

Country of ref document: HR

PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION HAS BEEN PUBLISHED

AC Divisional application: reference to earlier application

Ref document number: 2922846

Country of ref document: EP

Kind code of ref document: P

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: REQUEST FOR EXAMINATION WAS MADE

17P Request for examination filed

Effective date: 20191210

RBV Designated contracting states (corrected)

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

REG Reference to a national code

Ref country code: HK

Ref legal event code: DE

Ref document number: 40010074

Country of ref document: HK

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: EXAMINATION IS IN PROGRESS

17Q First examination report despatched

Effective date: 20210517

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: GRANT OF PATENT IS INTENDED

INTG Intention to grant announced

Effective date: 20211118

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE PATENT HAS BEEN GRANTED

GRAT Correction requested after decision to grant or after decision to maintain patent in amended form

Free format text: ORIGINAL CODE: EPIDOSNCDEC

AC Divisional application: reference to earlier application

Ref document number: 2922846

Country of ref document: EP

Kind code of ref document: P

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

RIN2 Information on inventor provided after grant (corrected)

Inventor name: ZHANG, YANLEI

Inventor name: SPERGEL, STEVEN H.

Inventor name: LIU, CHUNJIAN

Inventor name: LIN, SHUQUN

Inventor name: BATT, DOUGLAS G.

Inventor name: KUMAR, AMIT

Inventor name: TOKARSKI, JOHN S.

Inventor name: WROBLESKI, STEPHEN T.

Inventor name: WEINSTEIN, DAVID S.

Inventor name: MOSLIN, RYAN M.

RIN2 Information on inventor provided after grant (corrected)

Inventor name: ZHANG, YANLEI

Inventor name: SPERGEL, STEVEN H.

Inventor name: LIU, CHUNJIAN

Inventor name: LIN, SHUQUN

Inventor name: BATT, DOUGLAS G.

Inventor name: KUMAR, AMIT

Inventor name: TOKARSKI, JOHN S.

Inventor name: WROBLESKI, STEPHEN T.

Inventor name: WEINSTEIN, DAVID S.

Inventor name: MOSLIN, RYAN M.

REG Reference to a national code

Ref country code: CH

Ref legal event code: PK

Free format text: BERICHTIGUNG B8

REG Reference to a national code

Ref country code: AT

Ref legal event code: REF

Ref document number: 1486877

Country of ref document: AT

Kind code of ref document: T

Effective date: 20220515

REG Reference to a national code

Ref country code: NL

Ref legal event code: FP

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 602013081535

Country of ref document: DE

REG Reference to a national code

Ref country code: DK

Ref legal event code: T3

Effective date: 20220519

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: SE

Ref legal event code: TRGR

REG Reference to a national code

Ref country code: PT

Ref legal event code: SC4A

Ref document number: 3495358

Country of ref document: PT

Date of ref document: 20220602

Kind code of ref document: T

Free format text: AVAILABILITY OF NATIONAL TRANSLATION

Effective date: 20220526

REG Reference to a national code

Ref country code: ES

Ref legal event code: FG2A

Ref document number: 2914793

Country of ref document: ES

Kind code of ref document: T3

Effective date: 20220616

REG Reference to a national code

Ref country code: FI

Ref legal event code: FGE

REG Reference to a national code

Ref country code: RO

Ref legal event code: EPE

REG Reference to a national code

Ref country code: GR

Ref legal event code: EP

Ref document number: 20220401097

Country of ref document: GR

Effective date: 20220608

REG Reference to a national code

Ref country code: NO

Ref legal event code: T2

Effective date: 20220427

REG Reference to a national code

Ref country code: EE

Ref legal event code: FG4A

Ref document number: E022432

Country of ref document: EE

Effective date: 20220609

REG Reference to a national code

Ref country code: SK

Ref legal event code: T3

Ref document number: E 39964

Country of ref document: SK

REG Reference to a national code

Ref country code: HR

Ref legal event code: T1PR

Ref document number: P20220766

Country of ref document: HR

REG Reference to a national code

Ref country code: HU

Ref legal event code: AG4A

Ref document number: E059409

Country of ref document: HU

REG Reference to a national code

Ref country code: HR

Ref legal event code: ODRP

Ref document number: P20220766

Country of ref document: HR

Payment date: 20221103

Year of fee payment: 10

REG Reference to a national code

Ref country code: DE

Ref legal event code: R097

Ref document number: 602013081535

Country of ref document: DE

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed

Effective date: 20230130

P01 Opt-out of the competence of the unified patent court (upc) registered

Effective date: 20230418

REG Reference to a national code

Ref country code: HR

Ref legal event code: ODRP

Ref document number: P20220766

Country of ref document: HR

Payment date: 20231011

Year of fee payment: 11

REG Reference to a national code

Ref country code: HR

Ref legal event code: ODRP

Ref document number: P20220766

Country of ref document: HR

Payment date: 20241015

Year of fee payment: 12

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: LT

Payment date: 20241004

Year of fee payment: 12

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20241001

Year of fee payment: 12

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: MC

Payment date: 20241029

Year of fee payment: 12

Ref country code: NO

Payment date: 20241111

Year of fee payment: 12

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DK

Payment date: 20241118

Year of fee payment: 12

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: PL

Payment date: 20241007

Year of fee payment: 12

Ref country code: BE

Payment date: 20241007

Year of fee payment: 12

Ref country code: GR

Payment date: 20241014

Year of fee payment: 12

Ref country code: FI

Payment date: 20241121

Year of fee payment: 12

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20241001

Year of fee payment: 12

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: BG

Payment date: 20241017

Year of fee payment: 12

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: LV

Payment date: 20241003

Year of fee payment: 12

Ref country code: EE

Payment date: 20241003

Year of fee payment: 12

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: AT

Payment date: 20241025

Year of fee payment: 12

Ref country code: IS

Payment date: 20241008

Year of fee payment: 12

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: CZ

Payment date: 20241022

Year of fee payment: 12

Ref country code: HR

Payment date: 20241015

Year of fee payment: 12

Ref country code: IE

Payment date: 20241001

Year of fee payment: 12

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: RO

Payment date: 20241028

Year of fee payment: 12

Ref country code: SK

Payment date: 20241014

Year of fee payment: 12

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: IT

Payment date: 20241010

Year of fee payment: 12

Ref country code: ES

Payment date: 20241209

Year of fee payment: 12

Ref country code: RS

Payment date: 20241016

Year of fee payment: 12

Ref country code: SM

Payment date: 20241030

Year of fee payment: 12

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: SE

Payment date: 20241001

Year of fee payment: 12

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: MT

Payment date: 20241119

Year of fee payment: 12

Ref country code: CH

Payment date: 20241201

Year of fee payment: 12

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: TR

Payment date: 20241023

Year of fee payment: 12

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: AL

Payment date: 20241106

Year of fee payment: 12

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: CY

Payment date: 20241030

Year of fee payment: 12

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20250930

Year of fee payment: 13

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: SI

Payment date: 20251013

Year of fee payment: 13

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: MK

Payment date: 20241004

Year of fee payment: 12

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: LU

Payment date: 20251027

Year of fee payment: 13

Ref country code: NL

Payment date: 20251003

Year of fee payment: 13

REG Reference to a national code

Ref country code: HR

Ref legal event code: ODRP

Ref document number: P20220766

Country of ref document: HR

Payment date: 20251016

Year of fee payment: 13

REG Reference to a national code

Ref country code: CH

Ref legal event code: U11

Free format text: ST27 STATUS EVENT CODE: U-0-0-U10-U11 (AS PROVIDED BY THE NATIONAL OFFICE)

Effective date: 20251201

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: PT

Payment date: 20251107

Year of fee payment: 13

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: HU

Payment date: 20251105

Year of fee payment: 13